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ChemicalBook--->CAS DataBase List--->112726-66-6

112726-66-6

112726-66-6 Structure

112726-66-6 Structure
IdentificationBack Directory
[Name]

BTCP HCL
[CAS]

112726-66-6
[Synonyms]

gk13
GK 1
BTCP HCL
Benocyclidine
Benocyclidine hydrochloride
112726-66-6 BTCP HCL C19H25NS
BTCP HYDROCHLORIDE POTENT & SELECTIVE DO
Benzothiophenylcyclohexylpiperidine Maleate
1-(1-benzo(b)thien-2-ylcyclohexyl)-piperidin
1-(1-benzo(b)thien-2-ylcyclohexyl)piperidine
1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine
Piperidine,1-(1-benzo[b]thien-2-ylcyclohexyl)-
1-(1-Benzo[b]thiophen-2-ylcyclohexyl)piperidine
1-[1-(1-Benzothiophen-2-yl)cyclohexyl]piperidine
N-[1-(2-Benzo[b]thiophenyl)cyclohexyl]piperidine
1-[1-(1-benzothiophen-2-yl)cyclohexyl]piperidine Maleate
N-[1-(Benzo[b]thien-2-yl-cyclohexyl)]piperidine hydrochloride
[Molecular Formula]

C19H25NS
[MDL Number]

MFCD00153777
[MOL File]

112726-66-6.mol
[Molecular Weight]

299.47
Chemical PropertiesBack Directory
[Melting point ]

80℃ (ethanol )
[Boiling point ]

425.4±20.0 °C(Predicted)
[density ]

1.135±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

H2O: >180 mg/mL
[form ]

solid
[pka]

8.56±0.20(Predicted)
[color ]

white
Safety DataBack Directory
[RIDADR ]

UN 2811 6.1/PG 2
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Benzothiophenylcyclohexylpiperidine Maleate is a potent dopamine re-uptake/transport inhibitor different from PCP and other stimulants.
[Definition]

ChEBI: A tertiary amino compound that consists of cyclohexane having piperidin-1-yl and benzothiophen-2-yl groups attached at position 1. A potent dopamine re-uptake inhibitor with a behavioral profile different from that of phencyclidine (PCP) and similar to tha of cocaine.
[Biological Activity]

A potent dopamine re-uptake inhibitor with a behavioral profile different from that of PCP and similar to that of cocaine.
[References]

[1] vignon j, pinet v, cerruti c, et al. [3h] n-[1-(2-benzo (b) thiophenyl) cycohexyl] piperidine ([3h] btcp): a new phencyclidine analog selective for the dopamine uptake complex[j]. european journal of pharmacology, 1988, 148(3): 427-436.
[2] chaudieu i, vignon j, chicheportiche m, et al. role of the aromatic group in the inhibition of phencyclidine binding and dopamine uptake by pcp analogs[j]. pharmacology biochemistry and behavior, 1989, 32(3): 699-705.
[3] seeman p. brain dopamine receptors[j]. pharmacological reviews, 1980, 32(3): 229-313.
[4] maurice t, vignon j, kamenka j m, et al. in vivo labelling of the mouse dopamine uptake complex with the phencyclidine derivative [3 h] btcp[j]. neuroscience letters, 1989, 101(2): 234-238.
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